APDM Pharmaceuticals, a leader in pharmaceutical innovation, is hosting a walk-in interview on September 16, 2025, from 9:30 AM to 4:30 PM at its facility in Sakodara, Ahmedabad. We are seeking skilled professionals for Warehouse Manager, Quality Control (Officer/Sr. Officer, Executive/Sr. Executive), and Production (Operator, Officer/Executive) roles. Candidates with experience in cGMP, regulatory audits (USFDA, EU, MHRA, ANVISHA), and pharmaceutical operations are encouraged to apply. Join a dynamic team dedicated to creating a healthy future at APDM Pharmaceuticals!

Job Roles and Responsibilities

1. Warehouse Manager

• Oversee receipt, sampling, storage, and issuance of raw materials (RM), packing materials (PM), and finished goods (FG).
• Ensure material handling per SOPs and cGMP requirements (quarantine, approved, rejected, returned, expired).
• Maintain FIFO/FEFO systems and traceability of materials.
• Coordinate with production, QA, QC, and purchase for timely material availability.
• Ensure compliance during regulatory inspections (USFDA, EU, MHRA, WHO).
• Handle deviations, OOS, change controls, and CAPAs.
• Monitor stock levels to avoid overstocking or stock-outs, conducting physical stock verification.
• Analyze slow-moving, near-expiry, and obsolete materials, taking corrective actions.
• Maintain warehouse equipment (weighing balances, forklifts, temperature/humidity systems).
• Ensure audit-ready conditions and implement corrective actions post-audits.

2. Quality Control (Officer/Sr. Officer, Executive/Sr. Executive)

• Ensure compliance with cGMP, GLP, GDP, and SOPs in the QC laboratory.
• Perform analysis and release of raw materials, packing materials, in-process, and finished products.
• Handle laboratory QMS activities (Change Control, Deviation, OOS, OOT, Incidents).
• Conduct AMV, method verification, and method transfer activities.
• Manage calibration of laboratory instruments and coordinate with service providers.
• Procure chemicals, standards, columns, and consumables timely.
• Review and execute technology transfer documentation.
• Develop QC strategies aligned with regulatory guidelines (USFDA, EU, MHRA, ANVISHA).

3. Production (Operator, Officer/Executive)

• Operator (Compression):
  • Operate and monitor compression machines for tablet manufacturing.
  • Ensure proper machine setup, changeover, and shutdown per SOPs.
  • Adjust machine parameters to maintain product quality and yield.
  • Perform line clearance and in-process checks (weight, thickness, hardness, friability, disintegration).
  • Record activities in BMR and logbooks, adhering to cGMP and safety norms.
• Officer/Executive:
  • Execute production schedules and coordinate with stores, QA, QC, engineering, and planning.
  • Ensure timely availability of raw materials and consumables.
  • Maintain compliance with cGMP, SOPs, and regulatory requirements (USFDA, EU, MHRA, WHO).
  • Review BMRs, BPRs, and logbooks, handling deviations, change controls, and CAPAs.

Qualifications

• Warehouse Manager:
  • Education: B.Pharm, M.Pharm, B.Sc, or M.Sc.
  • Experience: 6–9 years in pharmaceutical warehouse management.
  • Skills: Expertise in cGMP, FIFO/FEFO, inventory management, regulatory audits (USFDA, EU, MHRA, ANVISHA), and equipment maintenance.
• Quality Control:
  • Education: M.Pharm or M.Sc.
  • Experience: 2–4 years (Officer/Sr. Officer), 4–6 years (Executive/Sr. Executive).
  • Skills: Proficiency in cGMP, GLP, GDP, QMS, AMV, method verification, and regulatory audits.
• Production:
  • Operator: ITI with 2–4 years in compression machine operations.
  • Officer/Executive: B.Pharm with 2–6 years in production.
  • Skills: Knowledge of cGMP, SOPs, BMR/BPR documentation, and regulatory compliance.
• Mandatory: Exposure to EU, MHRA, USFDA, and ANVISHA audits for all roles.

Benefits

• Competitive Salaries:
  • Warehouse Manager: INR 8,00,000–12,00,000/year.
  • Quality Control: INR 4,00,000–8,00,000/year (based on position and experience).
  • Production: INR 3,00,000–7,00,000/year (based on position and experience).
• Career Growth: Opportunities to advance in a leading pharmaceutical company.
• Work Environment: Collaborative, innovative, and focused on quality.
• Regulatory Exposure: Work with global standards (USFDA, EU, MHRA, WHO).
• Health Benefits: Comprehensive wellness programs for employees.

Application Instructions

Attend the walk-in interview on September 16, 2025, from 9:30 AM to 4:30 PM at:
Venue: Plot No. 775, 776 & 628, Vill.: Sakodara, Taluka Bavla, Ahmedabad, Gujarat-382220.
Requirements: Bring your resume and one passport-size photo.
For directions, scan the QR code in the job advertisement or visit Pharmabharat.com.

FAQs

Q: What documents are required for the walk-in interview?
A: Bring a resume highlighting relevant experience and regulatory audit exposure, along with one passport-size photo.

Q: Can candidates apply for multiple roles during the walk-in?
A: Yes, candidates meeting the qualifications for multiple roles can discuss their eligibility with the interview panel.